510(k) K884307

Device
Ivac(r) Volumetric Controller - Model 262
Applicant
Y
510(k) number
K884307
Product code
LDR
Decision
Substantially Equivalent (SESE)
Decision date
1988-11-01
Date received
1988-10-13
Regulation
880.5725
Classification name
Controller, Infusion, Intravascular, Electronic
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Third party reviewed
No

Related Records

Applicant Contact

Contact
KIMBERLY M CARLSON
Address
P.O. Box 85335 San Diego CA US 92138 92138

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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